Medical Director - Infectious Diseases. An opportunity to join the international team of Medical Directors sitting within a leading Clinical Research Organisation with multiple sites across the globe. Access to the whole drug development process and matrix management of project teams focused on trials related to infectious disease. This is an outstanding opportunity for an experienced MD from the Infectious Diseases area to join an industry-leading organisation
My client is a world leading global CRO. We are looking to recruit an experienced registered Oncologist (Medical Director) to provide medical, clinical and scientific advice, in all aspects of assigned studies. You will ideally have experience in a similar role within a Pharma or CRO environment.
My client is a world leading global CRO. We are looking to recruit an experienced registered Oncologist (Medical Director) to provide medical, clinical and scientific advice, in all aspects of assigned studies. You will ideally have experience in a similar role within a Pharma or CRO environment.
My client is a small niche biotechnology company who is seeking a Director Regulatory Affairs to manage the regulatory operations on a global level. You will report to the VP of the Regulatory group and hold significant regulatory experience on a international level. Ideally you will have gained experience working with innovative products (biologic) and previous leadership/managerial experience.
My client is a small niche biotechnology company who is seeking a Director Regulatory Affairs to manage the regulatory operations on a global level. You will report to the VP of the Regulatory group and hold significant regulatory experience on a international level. Ideally you will have gained experience working with innovative products (biologic) and previous leadership/managerial experience.
My client is a highly successful and expanding a Bio-Pharmaceutical company with an extensive pipeline and a high value commercial portfolio who is seeking a dynamic, innovative and highly motivated personality to take the lead for EU (and sometimes Global) Regulatory strategies and submissions. This role comes with an excellent salary; full–relocation package & excellent career prospects. Contact Theo Moore on +44 (0) 207 801 3384.
My client is a successful Brussels based Pharmaceutical Company focused on developing medicines for un-met medical needs, and continues to grow and develop at an extraordinary rate. They have ambitions to one day become a top ten pharmaceutical company and are offering fantastic opportunities to work on global development projects. Please contact Theo Moore on +44 (0)207 801 3380 or email your Cv in confidence to Theo@advregulatory.com
Please call one of Advanced's principals for Regulatory Affairs, Matt Greig or Theo Moore on +44 (0)207 801 3382 or +44 (0)7918 679 405. Alternatively you can email us directly on CV@AdvRegulatory.com
Take responsibility for a number of key projects. This high level strategic role will include providing input into the Global Regulatory Liaison for development strategy, submitting Clinical Trial Applications, project managing submission of Scientific Advice briefing packages & MAAs(or line extensions/Type II variations) for an expanding biotech company that has shown great levels of growth in the last 3 years. Contact Theo Moore CV@advregulatory.com
Please call one of Advanced's principals for Regulatory Affairs, Matt Greig or Theo Moore on +44 (0)207 801 3382 or +44 (0)7918 679 405. Alternatively you can email us directly on CV@AdvRegulatory.com
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